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1.
Minerva Med ; 88(3): 105-7, 1997 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-9105327

RESUMO

Meningeal carcinomatosis (MC) is an uncommon from of metastasis of solid tumors. We reported a clinical case of a woman with esophagus adenocarcinoma that a few months after surgical operation, presented episodes of vomiting, nausea, hypertension, mental change, unconsiousness; A contrast-enhanced CT of the brain revealed an "area of enhancement in the caudate nucleus" and cerebrospinal fluid cytologic studies evidenced the presence of carcinomatous cells. The clinical state of the patient deteriorated and she died a few days later. Autopsy confirmed meningeal carcinomatosis without parenchymal involvement.


Assuntos
Adenocarcinoma/secundário , Neoplasias Esofágicas/patologia , Neoplasias Meníngeas/secundário , Feminino , Humanos , Pessoa de Meia-Idade
2.
Ann Ital Med Int ; 10(2): 134-7, 1995.
Artigo em Italiano | MEDLINE | ID: mdl-7619654

RESUMO

Rhabdomyolysis is an acute skeletal muscle disorder characterized by altered integrity of the cell membranes of muscle fiber cells and can be caused by a variety of factors whose nature is not necessarily traumatic. Hypokalemia is one of the most common metabolic causes, accounting for about 14-28% of rhabdomyolytic syndromes. We report and discuss three cases of hypokalemia caused by diuretic treatment with hydrochlorothiazide: the main clinical features were muscle symptoms following massive rhabdomyolysis.


Assuntos
Hidroclorotiazida/efeitos adversos , Hipopotassemia/induzido quimicamente , Rabdomiólise/induzido quimicamente , Adulto , Ensaios Enzimáticos Clínicos , Creatina Quinase/sangue , Feminino , Seguimentos , Humanos , Hidroclorotiazida/administração & dosagem , Masculino , Pessoa de Meia-Idade , Rabdomiólise/diagnóstico , Fatores de Tempo
3.
Recenti Prog Med ; 87(12): 589-91, 1996 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-9066252

RESUMO

A young woman suffering from sideropenic anemia, bleeding disorders related to von Willebrand's disease and pulmonary vascular telangiectasias presented at our observation. Laboratory findings, genetic and hemostatic studies revealed platelet aggregation defect while in her father and grandfather lung angiodysplastic lesions without platelet aggregation defect. The association between bleeding disorders and pulmonary angiodysplasia has rarely presented in literature and deficiency of von Willebrand factor might increase the risk of bleeding in patients with coexisting angiodysplastic disease.


Assuntos
Malformações Arteriovenosas/diagnóstico , Pulmão/anormalidades , Pulmão/irrigação sanguínea , Telangiectasia Hemorrágica Hereditária/diagnóstico , Doenças de von Willebrand/diagnóstico , Anemia Ferropriva/diagnóstico , Anemia Ferropriva/genética , Malformações Arteriovenosas/genética , Feminino , Humanos , Masculino , Telangiectasia Hemorrágica Hereditária/genética , Doenças de von Willebrand/genética
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